Department of Plant Sciences, University of Western Ontario, London, Ontario, Canada.
Planta. 1972 Dec;103(4):281-301. doi: 10.1007/BF00386700.
In C. rubrum, the amount of flowering that is induced by a single dark period interrupting continuous light depends upon the duration of darkness. A rhythmic oscillation in sensitivity to the time that light terminates darkness regulates the level of flowering. The period length of this oscillation is close to 30 hours, peaks of the rhythm occurring at about 13, 43 and 73 h of darkness.Phasing of the rhythm by 6-, 12- and 18-h photoperiods was studied by exposing plants to a given photoperiod at different phases of the free-running oscillation in darkness. The shift in phase of the rhythm was then determined by varying the length of the dark period following the photoperiod; this dark period was terminated by continuous light.With a 6-h photoperiod the timing of both the light-on and light-off signals is shown to control rhythm phasing. However, when the photoperiod is increased to 12 or 18 h, only the light-off signal determines phasing of the rhythm. In prolonged periods of irradiation-12 to 62 h light-a "durational" response to light overrides any interaction between the timing of the light period and the position of the oscillation at which light is administered. Such prolonged periods of irradiation apparently suspend or otherwise interact with the rhythm so that, in a following dark period, it is reinitiated at a fixed phase relative to the time of the light-off signal to give a peak of the rhythm 13 h after the dusk signal.In daily photoperiodic cycles rhythm phasing by a 6-h photocycle was also estimated by progressively increasing the number of cycles given prior to a single dark period of varied duration.In confirmation of Bünning's (1936) hypothesis, calculated and observed phasing of the rhythm controlling flowering in c. rubrum accounts for the photoperiodic response of this species. Evidence is also discussed which indicates that the timing of disappearance of phytochrome Pfr may limit flowering over the early hours of darkness.
在 C. rubrum 中,单一暗期中断连续光照所诱导的开花量取决于暗期的持续时间。对光结束暗期的时间敏感性的节律性振荡调节开花水平。这种振荡的周期长度接近 30 小时,节律的峰值出现在暗期的 13、43 和 73 小时。通过将植物暴露在不同的自由运行暗期振荡相位下,用给定的光周期来研究节律的分相。然后通过改变光周期后的暗期长度来确定节律的相位变化;这个暗期被连续光照所终止。用 6 小时的光周期,光开和光关信号的时间都被证明可以控制节律的分相。然而,当光周期增加到 12 或 18 小时时,只有光关信号决定节律的分相。在长时间的辐照下(12 到 62 小时),对光的“持续时间”反应会覆盖光周期的时间和光施加的位置之间的任何相互作用。这种长时间的辐照显然会暂停或干扰节律,以至于在随后的暗期,它会相对于光关信号的时间在一个固定的相位重新开始,从而在黄昏信号后 13 小时出现节律的峰值。在每日光周期循环中,通过逐步增加在单个不同持续时间的暗期之前给予的周期数,也可以估计 6 小时光周期的节律分相。证实了 Bünning(1936)的假设,控制 C. rubrum 开花的节律分相计算和观察结果解释了该物种的光周期反应。还讨论了表明光敏色素 Pfr 消失的时间可能限制暗期早期开花的证据。